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elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil (Stribild®)


Reference No. 3616

Publication date:
20/02/2018


Appraisal information

elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil (Stribild®) 150 mg/150 mg/200 mg/245 mg film-coated tablet


Company: Gilead Sciences Ltd
BNF category: Infections
NMG meeting date: Not scheduled
AWMSG meeting date: Not scheduled
   
   
Submission Type: Nonsubmission
Status: Not endorsed
Advice No: Not available
Ratification by Welsh Government: 06/02/2018

Current Progress


Submission
received
NMG
meeting
AWMSG
meeting
Ratification by
Welsh Government

AWMSG advice

In the absence of a submission from the holder of the marketing authorisation, elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil (Stribild®) cannot be endorsed for use within NHS Wales for the treatment of HIV‑1 infection in adolescents aged 12 to < 18 years weighing ≥ 35 kg who are infected with HIV‑1 without known mutations associated with resistance to any of the three antiretroviral agents in Stribild® and who have experienced toxicities which preclude the use of other regimens that do not contain tenofovir disoproxil fumarate.
Statement of Advice (SOA)
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